JPH09501688A - 抗細菌性および抗汚れ性オキサチアジン類およびそれらの酸化物 - Google Patents
抗細菌性および抗汚れ性オキサチアジン類およびそれらの酸化物Info
- Publication number
- JPH09501688A JPH09501688A JP7507343A JP50734395A JPH09501688A JP H09501688 A JPH09501688 A JP H09501688A JP 7507343 A JP7507343 A JP 7507343A JP 50734395 A JP50734395 A JP 50734395A JP H09501688 A JPH09501688 A JP H09501688A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- alkyl
- phenyl
- compound
- antifouling
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 15
- 230000003373 anti-fouling effect Effects 0.000 title claims description 13
- AZHVQJLDOFKHPZ-UHFFFAOYSA-N oxathiazine Chemical class O1SN=CC=C1 AZHVQJLDOFKHPZ-UHFFFAOYSA-N 0.000 title description 5
- -1 tetrahydropyranyloxy, phenoxy Chemical group 0.000 claims abstract description 45
- 239000000203 mixture Substances 0.000 claims abstract description 38
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 19
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 11
- 239000001257 hydrogen Substances 0.000 claims abstract description 11
- 125000001424 substituent group Chemical group 0.000 claims abstract description 10
- 125000002541 furyl group Chemical group 0.000 claims abstract description 7
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 7
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims abstract description 6
- 125000001544 thienyl group Chemical group 0.000 claims abstract description 6
- 125000004953 trihalomethyl group Chemical group 0.000 claims abstract description 6
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims abstract description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 5
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims abstract description 4
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 claims abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 4
- 229910052717 sulfur Chemical group 0.000 claims abstract description 4
- 239000011593 sulfur Chemical group 0.000 claims abstract description 4
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims abstract description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims abstract description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 3
- 125000006518 morpholino carbonyl group Chemical group [H]C1([H])OC([H])([H])C([H])([H])N(C(*)=O)C1([H])[H] 0.000 claims abstract description 3
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 3
- 239000001301 oxygen Substances 0.000 claims abstract description 3
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 7
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract 4
- 125000001475 halogen functional group Chemical group 0.000 claims abstract 4
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 29
- 239000004480 active ingredient Substances 0.000 claims description 26
- 239000000126 substance Substances 0.000 claims description 18
- 244000005700 microbiome Species 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 14
- 241000894006 Bacteria Species 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000000654 additive Substances 0.000 claims description 10
- 239000011248 coating agent Substances 0.000 claims description 10
- 239000003973 paint Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000008199 coating composition Substances 0.000 claims description 6
- 238000003860 storage Methods 0.000 claims description 6
- 239000002023 wood Substances 0.000 claims description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 229920000180 alkyd Polymers 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- 239000000417 fungicide Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- 239000003899 bactericide agent Substances 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 claims description 3
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- 239000000178 monomer Substances 0.000 claims description 3
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- 239000011347 resin Substances 0.000 claims description 3
- 239000002689 soil Substances 0.000 claims description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- 239000012963 UV stabilizer Substances 0.000 claims description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 150000004808 allyl alcohols Chemical class 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 230000001580 bacterial effect Effects 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 claims description 2
- 230000007797 corrosion Effects 0.000 claims description 2
- 239000006184 cosolvent Substances 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 239000005007 epoxy-phenolic resin Substances 0.000 claims description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003112 inhibitor Substances 0.000 claims description 2
- 239000002917 insecticide Substances 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 239000011505 plaster Substances 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 229920000647 polyepoxide Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- QXMAXBCUOKUJJZ-UHFFFAOYSA-N 3-(4-chlorophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound C1=CC(Cl)=CC=C1C1=NOCCS1 QXMAXBCUOKUJJZ-UHFFFAOYSA-N 0.000 claims 1
- 230000001464 adherent effect Effects 0.000 claims 1
- 239000003623 enhancer Substances 0.000 claims 1
- 230000014759 maintenance of location Effects 0.000 claims 1
- 229920002239 polyacrylonitrile Polymers 0.000 claims 1
- 239000005871 repellent Substances 0.000 claims 1
- 230000002940 repellent Effects 0.000 claims 1
- 239000012748 slip agent Substances 0.000 claims 1
- 239000002519 antifouling agent Substances 0.000 abstract description 3
- 230000001098 anti-algal effect Effects 0.000 abstract 1
- 230000000656 anti-yeast Effects 0.000 abstract 1
- 125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 abstract 1
- 230000002013 molluscicidal effect Effects 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 9
- 125000005843 halogen group Chemical group 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- 238000009472 formulation Methods 0.000 description 6
- 230000012010 growth Effects 0.000 description 6
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- 239000000843 powder Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 241000195493 Cryptophyta Species 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
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- 239000004094 surface-active agent Substances 0.000 description 4
- 241000238424 Crustacea Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
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- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 2
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- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 2
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- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 201000010153 skin papilloma Diseases 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- DFNPRTKVCGZMMC-UHFFFAOYSA-M tributyl(fluoro)stannane Chemical compound CCCC[Sn](F)(CCCC)CCCC DFNPRTKVCGZMMC-UHFFFAOYSA-M 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical class CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- LHHPEAQVCCPLBC-UHFFFAOYSA-N tributyltin;hydrate Chemical compound O.CCCC[Sn](CCCC)CCCC LHHPEAQVCCPLBC-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D419/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
- C07D419/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D419/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D291/00—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
- C07D291/02—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms not condensed with other rings
- C07D291/06—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Materials Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.細菌もしくは汚染性微生物、またはそれらの生息場所に、抗細菌的または抗 汚染性微生物的に有効な量の式 [式中、nは0、または2であり、R1は水素、C1-4アルキルまたはベンジルで あり、そしてRは (a)フェニル;ヒドロキシル、ハロ、C1-12アルキル、C5-6シクロアルキル 、トリハロメチル、フェニル、C1-5アルコキシ、C1-5アルキルチオ、テトラヒ ドロピラニルオキシ、フェノキシ、C2-4アルキルカルボニル、フェニルカルボ ニル、C1-4アルキルスルフィニル、C1-4アルキルスルホニル、カルボキシもし くはそのアルカリ金属塩、C1-4アルキルオキシカルボニル、C1-4アルキルアミ ノカルボニル、フェニルアミノカルボニル、トリルアミノカルボニル、モルホリ ノカルボニル、アミノ、ニトロ、シアノ、ジオキソラニルまたはC1-4アルキル オキシイミノメチルから独立して選択される1〜3個の置換基で置換されたフェ ニル;ナフチル;ピリジニル;好適にはnが2でない時の、チエニル;フラニル ;またはC1-4アルキル、C1-4アルキルオキシ、C1-4アルキルチオ、ハロ、シ アノ、ホルミル、アセチル、ベンゾイル、ニトロ、C1-4アルキルオキシカルボ ニル、フェニル、フェニルアミノカルボニルおよびC1-4アルキルオキシイミノ メチルから独立して選択される1〜3個の置換基で置換されたチエニルもしくは フラニルを表すか、或いはRは式 (b) の基を表し、 ここでXは酸素または硫黄であり、Yは窒素、CHまたはC(C1-4アルキルオキ シ)であり、そしてR″は水素またはC1-4アルキルである] を有する化合物を投与することを含んでなる、細菌および汚染性微生物を抑制す る方法。 2.抗細菌的または抗汚染性微生物的に有効な量の式(I)の化合物を表面に適 用するかまたは木材以外の無生命物質もしくは該無生命物質から製造されるかも しくはそれにより覆われた物体の表面に適用するかまたは該物質もしくは物体中 に導入することを含んでなる、木材以外の無生命物質、および該無生命物質から 製造されるかまたはそれにより覆われた物体を保護する請求の範囲第1項に従う 方法。 3.式(I)の化合物が5,6−ジヒドロ−3−(2−チエニル)−1,4,2−オ キサチアジン,4−オキシドまたは3−(4−クロロフェニル)−5,6−ジヒドロ −1,4,2−オキサチアジン,4,4−ジオキシドである、請求の範囲第2項に従 う方法。 4.無生命物質が付着性コーテイング物質、例えばペイント、抗汚れ性ペイント 、ワニス、ラッカー、仕上げ剤またはしっくいである、請求の範囲第2項に従う 方法。 5.付着性コーテイング物質が貯蔵容器中に保存されているかまたはコーテイン グ物質がフィルム状で基質に適用されている、請求の範囲第4 項に従う方法。 6.水中の物体、例えば船体、港設備、乾ドック、水門、閘門、係留塔、ブイ、 掘穿台、橋、パイプライン、釣り網、ケーブルおよび水と常にまたは頻繁に接触 する他の物体に抗汚れ有効量の請求の範囲第1項で定義されている式(I)の化 合物を含んでなる抗汚れ組成物を適用することを含んでなる、該物体を保護する ための請求の範囲第2項に従う方法。 7.式(I)の化合物の量が組成物の合計重量に基づいて0.001〜95重量 %の範囲である、請求の範囲第2項に従う方法。 8.(a)活性成分としての請求の範囲第1項で定義されている通りの式(I) の化合物、および (b)例えばジアルキルシロキサン類、(メタ)アクリル酸、(メタ)アクリル 酸エステル類、ビニルおよびアリルアルコール類並びに誘導されたエステル類、 マレイン酸、スチレン、塩化ビニル、ブタジエン、アクリルアミド、アクリロニ トリルの如き単量体から誘導される重合体または共重合体、または例えばアルキ ド樹脂、ポリウレタン、エポキシ樹脂、フェノール系樹脂およびウレア−ホルム アルデヒド樹脂の如き樹脂 を含んでなるコーテイング組成物。 9.撥水剤、表面滑り剤、有機結合剤、殺昆虫剤、殺菌・殺カビ剤、殺細菌剤、 補助溶媒、加工添加剤、揮発保留剤、可塑剤、紫外線安定剤または安定性増加剤 、染料、カラー顔料、乾燥剤、腐食抑制剤、抗沈降剤、抗皮張り剤、および抗発 泡剤よりなる群から選択される1種もしくはそれ以上の添加剤をさらに含んでな る、請求の範囲第8項に従うコーテイング組成物。 10.該抗汚れペイント組成物の乾燥分の合計重量に基づいて10%〜 75重量%までの活性成分を含んでなる、請求の範囲第8項に従う抗汚れペイン ト組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US11135293A | 1993-08-24 | 1993-08-24 | |
US111,352 | 1993-08-24 | ||
PCT/EP1994/002784 WO1995005739A1 (en) | 1993-08-24 | 1994-08-24 | Antibacterial and antifouling oxathiazines and their oxides |
Publications (2)
Publication Number | Publication Date |
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JPH09501688A true JPH09501688A (ja) | 1997-02-18 |
JP3665335B2 JP3665335B2 (ja) | 2005-06-29 |
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JP50734395A Expired - Fee Related JP3665335B2 (ja) | 1993-08-24 | 1994-08-24 | 抗細菌性および抗汚れ性オキサチアジン類およびそれらの酸化物 |
Country Status (31)
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US (2) | US5712275A (ja) |
EP (1) | EP0715495B1 (ja) |
JP (1) | JP3665335B2 (ja) |
KR (1) | KR100342363B1 (ja) |
CN (2) | CN100369905C (ja) |
AP (2) | AP568A (ja) |
AT (1) | ATE163836T1 (ja) |
AU (1) | AU680294B2 (ja) |
BR (1) | BR9407567A (ja) |
CY (1) | CY2089B1 (ja) |
CZ (1) | CZ286710B6 (ja) |
DE (1) | DE69408998T2 (ja) |
DK (1) | DK0715495T3 (ja) |
ES (1) | ES2113674T3 (ja) |
FI (1) | FI112434B (ja) |
GR (1) | GR3026333T3 (ja) |
HK (1) | HK1006054A1 (ja) |
HU (1) | HU214846B (ja) |
MX (1) | MX9406466A (ja) |
MY (1) | MY111021A (ja) |
NO (1) | NO315181B1 (ja) |
NZ (1) | NZ273306A (ja) |
OA (1) | OA10266A (ja) |
PL (1) | PL185409B1 (ja) |
RO (1) | RO116243B1 (ja) |
RU (1) | RU2143805C1 (ja) |
SG (1) | SG66277A1 (ja) |
SK (1) | SK282008B6 (ja) |
TW (1) | TW304159B (ja) |
WO (1) | WO1995005739A1 (ja) |
ZA (1) | ZA946449B (ja) |
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CA1273921A (en) * | 1982-09-28 | 1990-09-11 | Walter G. Brouwer | 3-aryl-5, 6-dihydro-1, 4, 2-oxathiazines and their oxides |
US4569690A (en) * | 1982-09-28 | 1986-02-11 | Uniroyal, Inc. | 3-Aryl-5,6-dihydro-1,4,2-oxathiazines and their oxides |
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1994
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Cited By (7)
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JP2005507429A (ja) * | 2001-11-08 | 2005-03-17 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 4−ブロモ−2−(4−クロロフェニル)−5−(トリフルオロメチル)−1h−ピロール−3−カルボニトリルを含む相乗性防汚組成物 |
JP4666914B2 (ja) * | 2001-11-08 | 2011-04-06 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 4−ブロモ−2−(4−クロロフェニル)−5−(トリフルオロメチル)−1h−ピロール−3−カルボニトリルを含む相乗性防汚組成物 |
JP2006063029A (ja) * | 2004-08-27 | 2006-03-09 | Api Corporation | 水棲汚損生物付着防止剤組成物 |
JP4489535B2 (ja) * | 2004-08-27 | 2010-06-23 | ベニートヤマ株式会社 | 水棲汚損生物付着防止剤組成物 |
JP2008533220A (ja) * | 2005-03-03 | 2008-08-21 | ワッカー ケミー アクチエンゲゼルシャフト | 有機ケイ素化合物を基礎とする架橋可能なコンパウンド |
JP2006282555A (ja) * | 2005-03-31 | 2006-10-19 | Katayama Chem Works Co Ltd | 工業用抗菌剤およびそれを用いた工業的抗菌方法 |
JP2010522796A (ja) * | 2007-03-27 | 2010-07-08 | ダニスコ エイ/エス | 組成物 |
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